Prokopenko S N, Brumby A, O'Keefe L, Prior L, He Y, Saint R, Bellen H J
Program in Developmental Biology, Baylor College of Medicine, Houston, Texas 77030 USA.
Genes Dev. 1999 Sep 1;13(17):2301-14. doi: 10.1101/gad.13.17.2301.
Cytokinesis ensures the successful completion of the cell cycle and distribution of chromosomes, organelles, and cytoplasm between daughter cells. It is accomplished by formation and constriction of an actomyosin contractile ring that drives the progression of a cleavage furrow. Microinjection experiments and in vitro transfection assays have suggested a requirement for small GTPases of the Rho family in cytokinesis. Yet, the identity of proteins regulating Rho signaling pathways during cytokinesis remains unknown. Here we show that in Drosophila, Pebble (Pbl), a putative exchange factor for Rho GTPases (RhoGEF), is required for the formation of the contractile ring and initiation of cytokinesis. The dynamics of Pbl expression and its distribution during mitosis, as well as structure-function analysis, indicate that it is a key regulatory component of the pathway. pbl interacts genetically with Rho1, but not with Rac1 or Cdc42, and Pbl and Rho1 proteins interact in vivo in yeast. Similar to mutations in pbl, loss of Rho1 or expression of a dominant-negative Rho1 blocks cytokinesis. Our results identify Pbl as a RhoGEF specifically required for cytokinesis and linked through Rho1 activity to the reorganization of the actin cytoskeleton at the cleavage furrow.
胞质分裂确保细胞周期的成功完成以及染色体、细胞器和细胞质在子细胞之间的分配。它通过形成和收缩肌动球蛋白收缩环来实现,该收缩环驱动分裂沟的进展。显微注射实验和体外转染分析表明,胞质分裂需要Rho家族的小GTP酶。然而,在胞质分裂过程中调节Rho信号通路的蛋白质的身份仍然未知。在这里,我们表明,在果蝇中,Pebble(Pbl),一种假定的Rho GTP酶交换因子(RhoGEF),是收缩环形成和胞质分裂起始所必需的。Pbl在有丝分裂期间的表达动态及其分布,以及结构功能分析表明,它是该信号通路的关键调节成分。pbl与Rho1发生遗传相互作用,但不与Rac1或Cdc42相互作用,并且Pbl和Rho1蛋白在酵母中在体内相互作用。与pbl中的突变类似,Rho1的缺失或显性负性Rho1的表达会阻断胞质分裂。我们的结果确定Pbl是胞质分裂特异性所需的RhoGEF,并通过Rho1活性与分裂沟处肌动蛋白细胞骨架的重组相关联。